Thrombotic thrombocytopenic purpura in childhood
Author:
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.22094/fullpdf
Reference48 articles.
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2. Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and hemolytic-uremic syndrome;Furlan;N Engl J Med,1998
3. Case series of thrombotic thrombocytopenic purpura in children and adolescents;Horton;J Pediatr Hematol Oncol,2003
4. The incidence of thrombotic thrombocytopenic purpura-hemolytic syndrome: All patients, idiopathic patients, and patients with severe ADAMTS13 deficiency;Terrell;J Thromb Haemost,2005
5. ADAMTS 13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: Relation to presenting features and clinical outcomes in a prospective cohort of 142 patients;Vesely;Blood,2003
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1. Hematology of Childhood and Adolescence;Reference Module in Biomedical Sciences;2021
2. Novel homozygous ADAMTS13 mutation with neonatal presentation of congenital thrombotic thrombocytopenic purpura in two Indian origin babies;Pediatric Hematology Oncology Journal;2019-03
3. Acquired thrombotic thrombocytopenic purpura in a child: rituximab to prevent relapse. A pediatric report and literature review;Haematologica;2018-02-28
4. Child-onset and adolescent-onset acquired thrombotic thrombocytopenic purpura with severe ADAMTS13 deficiency: a cohort study of the French national registry for thrombotic microangiopathy;The Lancet Haematology;2016-11
5. Disorders of Platelets;Lanzkowsky's Manual of Pediatric Hematology and Oncology;2016
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